DNA binding;
NMR;
protein dynamics;
SIX1;
transcription factor;
N-TERMINAL DOMAIN;
IV E SUBUNIT;
TRANSCRIPTION FACTORS;
BACKBONE DYNAMICS;
PROTEIN BACKBONE;
TORSION ANGLES;
6;
FAMILY;
NMR;
APOPTOSIS;
COMPLEX;
D O I:
10.1002/psc.3376
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Human sine oculis homeobox homolog (SIX) 1 contains a homeodomain (HD), which is important for binding to DNA. In this study, we carried out structural studies on the HD of human SIX1 using nuclear magnetic resonance (NMR) spectroscopy. Its secondary structures and dynamics in solution were explored. HD is well-structured in solution, and our study shows that it contains three alpha-helices. Dynamics study indicates that the N- and C-terminal residues of HD are flexible in solution. HD of human SIX1 exhibits molecular interactions with a short double-strand DNA sequence evidenced by the H-1-N-15-heteronuclear single quantum correlation (HSQC) and F-19-NMR experiments. Our current study provides structural information for HD of human SIX1. Further studies indicate that this construct can be utilized to study SIX1 and DNA interactions.